Twist Lancet(30G)

GUDID 56949517070887

Sterile Lancet for Single Use (Box of 100 lancets), sterilized with Irradiation sterilization

Shandong Lianfa Medical Plastic Products CO.,LTD

Blood lancet, single-use

• Primary Device ID: 56949517070887
• NIH Device Record Key: 4387498f-9eb6-4016-95cf-53cb712b101c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Twist Lancet(30G)
• Version Model Number: LF-TL-30
• Company DUNS: 421330121
• Company Name: Shandong Lianfa Medical Plastic Products CO.,LTD
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06949517008021 [Primary]
GS1	56949517070887 [Unit of Use]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K222472

FDA Product Code

• QRL: Multiple Use Blood Lancet For Single Patient Use Only

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-11
• Device Publish Date: 2024-11-01

On-Brand Devices [Twist Lancet(30G)]

• 56949517070689: Sterile Lancet for Single Use (Box of 500 lancets), rediation(gamma) sterilization
• 56949517070665: Sterile Lancet for Single Use (Box of 500 lancets), sterilized with Ethylene Oxide
• 56949517070658: Sterile Lancet for Single Use (Box of 150 lancets), sterilized with Ethylene Oxide
• 56949517070887: Sterile Lancet for Single Use (Box of 100 lancets), sterilized with Irradiation sterilization